Canonical Allele Identifier: PA2573100966
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1331736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1780Gly
CA352141409
NM_198056.3:c.5339A>G